# K140352: Veraplug

- Pathway: 510(k) (Traditional)
- Applicant: Krishna Imports Inc Dba Stephens Instruments
- Decided: Nov 13, 2014 after 274 days
- Product code: LZU (Plug, Punctum)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K972523 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972523: Punctual Occluder, Odyssey Medical, Inc. (1997) Summary page 4.

## Indications for use
The VeraPlug™ Punctal Plug is for use in patients with dry eye syndromes.

Source page: https://510kreport.com/device/K140352
Methodology: https://510kreport.com/methodology